Rare TP53 variant associated with Li-Fraumeni syndrome exhibits variable penetrance in a Saudi familyRare TP53 variant associated with Li-Fraumeni syndrome exhibits variable

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Gliomas arising in the setting of Li-Fraumeni syndrome stratify into two molecular subgroups with divergent clinicopathologic featuresUCSF UC San Francisco Previously Published

gf15417912 42..49Overview of the Clinical Features of Li-Fraumeni Syndrome and the Current European ERN GENTURIS Guideline Übersicht über die klinischen Merkmale

GUIDELINES FOR THE LI-FRAUMENI AND HERITABLE TP53-RELATED CANCER SYNDROMES Guidelines for the identification of individuals who should be tested for germline disease-causing

Case Report Diagnostic Genetics A Case of Late-Onset Li-Fraumeni–like Syndrome with Unilateral Breast Cancer Yonggeun Cho, M.D.1, Juwon Kim, M.D.1, Yoonjung Kim, M.D.1,

Registry Protocol Division of Pediatric Neurooncology Department of Pediatric Hematology and Oncology Heidelberg University Hospital Germany Email: [email protected] 2 ACC

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Citación provisional: Ossa CA, Molina G, Cock-Rada AM. Síndrome de Li-Fraumeni: reporte de un caso y revisión de la literatura. Biomédica. 2016;36(3).